Canonical Allele Identifier: CA772624009

Gene: CHRNE C17orf107

Linked Data

• dbSNP Id: rs1273944818
• MyVariant Identifiers: chr17:g.4802716A>G (hg19) ; chr17:g.4899421A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.4899421A>G , CM000679.2:g.4899421A>G	GRCh38
NC_000017.10:g.4802716A>G , CM000679.1:g.4802716A>G	GRCh37
NC_000017.9:g.4743495A>G	NCBI36
NG_008029.2:g.8655T>C
NG_028005.1:g.71082A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000649488.2:c.1033-37T>C (CHRNE) MANE Select	ENSP00000497829.1:n.1033-37T>C
ENST00000649830.1:c.100-37T>C (CHRNE)	ENSP00000496907.1:n.100-37T>C
ENST00000652550.1:n.763-37T>C (CHRNE)
ENST00000293780.4:c.1033-37T>C (CHRNE)	ENSP00000293780.4:n.1033-37T>C
ENST00000521575.1:c.-342A>G (C17orf107)	ENSP00000429241.1:n.-342A>G
ENST00000572438.1:n.719-37T>C (CHRNE)
NM_000080.3:c.1033-37T>C (CHRNE)	NP_000071.1:n.1033-37T>C
NM_000080.4:c.1033-37T>C (CHRNE) MANE Select	NP_000071.1:n.1033-37T>C
XM_017024115.1:c.997-37T>C (CHRNE)	XP_016879604.1:n.997-37T>C
XR_001752421.1:n.1763-37T>C (CHRNE)